Construction of Cellulose Binding Domain Fusion FMN-Dependent NADH-Azoreductase and Glucose 1-Dehydrogenase for the Development of Flow Injection Analysis with Fusion Enzymes Immobilized on Cellulose

The cellulose binding domain (CBD) of cellulosome-integrating protein A from Clostridium thermocellum NBRC 103400 was genetically fused to FMN-dependent NADH-azoreductase (AZR) and glucose 1-dehydrogenase (GDH) from Bacillus subtilis. The fusion enzymes, AZR-CBD and CBD-GDH, were expressed in Escher...

Full description

Saved in:
Bibliographic Details
Published inJournal of applied glycoscience : JAG Vol. 66; no. 2; p. 65
Main Authors Yano, Shigekazu, Hori, Yukari, Kijima, Tatsuro, Konno, Hiroyuki, Suyotha, Wasana, Takagi, Kazuyoshi, Wakayama, Mamoru
Format Journal Article
LanguageJapanese
Published Tsukuba Japan Science and Technology Agency 01.01.2019
Subjects
Online AccessGet full text
ISSN1344-7882
1880-7291
DOI10.5458/jag.jag.JAG-2018_0011

Cover

Abstract The cellulose binding domain (CBD) of cellulosome-integrating protein A from Clostridium thermocellum NBRC 103400 was genetically fused to FMN-dependent NADH-azoreductase (AZR) and glucose 1-dehydrogenase (GDH) from Bacillus subtilis. The fusion enzymes, AZR-CBD and CBD-GDH, were expressed in Escherichia coli Rosetta-gami B (DE3). The enzymes were purified from cell-free extracts, and the specific activity of AZR-CBD was 15.1 U/mg and that of CBD-GDH was 22.6 U/mg. AZR-CBD and CBD-GDH bound strongly to 0.5 % swollen cellulose at approximately 95 and 98 % of the initial protein amounts, respectively. After immobilization onto the swollen cellulose, AZR-CBD and CBD-GDH retained their catalytic activity. Both enzymes bound weakly to 0.5 % microcrystalline cellulose, but the addition of a high concentration of microcrystalline cellulose (10 %) improved the binding rate of both enzymes. A reactor for flow injection analysis was filled with microcrystalline cellulose-immobilized AZR-CBD and CBD-GDH. This flow injection analysis system was successfully applied for the determination of glucose, and a linear calibration curve was observed in the range of approximately 0.16–2.5 mM glucose, with a correlation coefficient, r, of 0.998.
AbstractList The cellulose binding domain (CBD) of cellulosome-integrating protein A from Clostridium thermocellum NBRC 103400 was genetically fused to FMN-dependent NADH-azoreductase (AZR) and glucose 1-dehydrogenase (GDH) from Bacillus subtilis. The fusion enzymes, AZR-CBD and CBD-GDH, were expressed in Escherichia coli Rosetta-gami B (DE3). The enzymes were purified from cell-free extracts, and the specific activity of AZR-CBD was 15.1 U/mg and that of CBD-GDH was 22.6 U/mg. AZR-CBD and CBD-GDH bound strongly to 0.5 % swollen cellulose at approximately 95 and 98 % of the initial protein amounts, respectively. After immobilization onto the swollen cellulose, AZR-CBD and CBD-GDH retained their catalytic activity. Both enzymes bound weakly to 0.5 % microcrystalline cellulose, but the addition of a high concentration of microcrystalline cellulose (10 %) improved the binding rate of both enzymes. A reactor for flow injection analysis was filled with microcrystalline cellulose-immobilized AZR-CBD and CBD-GDH. This flow injection analysis system was successfully applied for the determination of glucose, and a linear calibration curve was observed in the range of approximately 0.16–2.5 mM glucose, with a correlation coefficient, r, of 0.998.
Author Suyotha, Wasana
Wakayama, Mamoru
Kijima, Tatsuro
Yano, Shigekazu
Hori, Yukari
Takagi, Kazuyoshi
Konno, Hiroyuki
Author_xml – sequence: 1
  givenname: Shigekazu
  surname: Yano
  fullname: Yano, Shigekazu
– sequence: 2
  givenname: Yukari
  surname: Hori
  fullname: Hori, Yukari
– sequence: 3
  givenname: Tatsuro
  surname: Kijima
  fullname: Kijima, Tatsuro
– sequence: 4
  givenname: Hiroyuki
  surname: Konno
  fullname: Konno, Hiroyuki
– sequence: 5
  givenname: Wasana
  surname: Suyotha
  fullname: Suyotha, Wasana
– sequence: 6
  givenname: Kazuyoshi
  surname: Takagi
  fullname: Takagi, Kazuyoshi
– sequence: 7
  givenname: Mamoru
  surname: Wakayama
  fullname: Wakayama, Mamoru
BookMark eNo9kMtOwzAQRS0EEs9PQLLEOuBxktpZhpaWIiib7isnnrSuHLvECVX7g_wWiXgsRjOax7lXc0lOnXdIyC2w-zRJ5cNWre-HeMlnEWcgV4wBnJALkJJFgmdw2tdxkkRCSn5ObkIwBWNpxiDjcEG-xt6FtunK1nhHfUXHaG1nfUD6aJw2bk0nvlbG0WkXhpXp2yKa4A6dRtfSRT55jvKjb1D3CNVfKafpzHblQIB-c3PQjV-jG2aVb2i7QTrBT7R-Vw-EXnJq_Z7O3RZ_TORO2UMwge5Nu_mTfXLHQ42BzuvaF8aaI2rat__dXpOzStmAN7_5iiynT8vxc_T6PpuP89doC-koiTLghchKGBWMiziFChWroKgE9P_AUlaxZighFkqoTHAsRkKXUiPIisk0ia_I3Q921_iPDkO72vqu6Q2HFedJGo8yKZP4G2FtgOY
ContentType Journal Article
Copyright Copyright Japan Science and Technology Agency 2019
Copyright_xml – notice: Copyright Japan Science and Technology Agency 2019
DBID 7QO
8FD
FR3
P64
DOI 10.5458/jag.jag.JAG-2018_0011
DatabaseName Biotechnology Research Abstracts
Technology Research Database
Engineering Research Database
Biotechnology and BioEngineering Abstracts
DatabaseTitle Engineering Research Database
Biotechnology Research Abstracts
Technology Research Database
Biotechnology and BioEngineering Abstracts
DatabaseTitleList Engineering Research Database
DeliveryMethod fulltext_linktorsrc
Discipline Anatomy & Physiology
EISSN 1880-7291
GroupedDBID 2WC
7QO
8FD
ACIWK
ACPRK
AFRAH
ALMA_UNASSIGNED_HOLDINGS
DU5
FR3
JSF
JSH
KQ8
OK1
P64
PGMZT
RJT
RPM
RZJ
ID FETCH-LOGICAL-j1564-912b79c16b027351fea0f1bf71019ec8f3d0e8137a7a972eb67dc8de18f08543
ISSN 1344-7882
IngestDate Mon Jun 30 12:07:02 EDT 2025
IsPeerReviewed false
IsScholarly true
Issue 2
Language Japanese
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-j1564-912b79c16b027351fea0f1bf71019ec8f3d0e8137a7a972eb67dc8de18f08543
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
PQID 2245369884
PQPubID 2048451
ParticipantIDs proquest_journals_2245369884
PublicationCentury 2000
PublicationDate 20190101
PublicationDateYYYYMMDD 2019-01-01
PublicationDate_xml – month: 01
  year: 2019
  text: 20190101
  day: 01
PublicationDecade 2010
PublicationPlace Tsukuba
PublicationPlace_xml – name: Tsukuba
PublicationTitle Journal of applied glycoscience : JAG
PublicationYear 2019
Publisher Japan Science and Technology Agency
Publisher_xml – name: Japan Science and Technology Agency
SSID ssib005901921
ssj0046186
Score 2.1426318
Snippet The cellulose binding domain (CBD) of cellulosome-integrating protein A from Clostridium thermocellum NBRC 103400 was genetically fused to FMN-dependent...
SourceID proquest
SourceType Aggregation Database
StartPage 65
SubjectTerms Azoreductase
Binding
Catalysis
Catalytic activity
Cellulose
Correlation coefficient
Correlation coefficients
Crystalline cellulose
Dehydrogenase
Dehydrogenases
E coli
Enzymes
Flow injection analysis
Glucose
Glucose 1-dehydrogenase
Immobilization
Injection
NADH
Nicotinamide adenine dinucleotide
Protein A
Proteins
Title Construction of Cellulose Binding Domain Fusion FMN-Dependent NADH-Azoreductase and Glucose 1-Dehydrogenase for the Development of Flow Injection Analysis with Fusion Enzymes Immobilized on Cellulose
URI https://www.proquest.com/docview/2245369884
Volume 66
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lj9MwELZ2Fw5cELAgHgvyAXGpssRNmjjHQltKtVsOZKXuqXISp5u-InUTofYP8reYsZ00-wABh0SVXXUsz9eZ8XgehLy3o5ilSce2kjaLLbBvmcV5mlqeLaTPvSBII0xOPh97wwt3NOlMDg4fNqKWyiI6jXf35pX8D1dhDPiKWbL_wNn6R2EAPgN_4Q0chvdf8Ri7bVb1X1VchVwuyyVGoH_KdLZKL1_B0b81KNEp1hqcj62e6XpbtMbd3tDq7vINVm8tQJupi4QvJoadwTevtskmB-o4V4UjNqKMkORgmf8AITOXehF1jRPl3zVk--vdFmtCfYWdwVjcHRi5MFyv9jcGsjAG8my5jfMq_Qg9GKNu3RDsUqjW4a3vV9lMLsSurGGa6xT6y3IhNtk-0mCerZS5HIriutzk9QR23VZqONvk23KRNb0hmIB1wxsyAgtjLxZx1_Y3FK2uymZtCHvHdTGaUmsDqcdAnmF7X9bUELovjPkntBviXre5uK2F8C5SdT-YneIDmwKoZVyFD-7VbhVqMP42HVycnU3D_iQ8JA_avq_CDZpeJ8wPVmXrtIXhYo8D5Ugw69eZaUj2471E79gZyngKn5DHhqm0qyH8lBzMxTNyDGAp8tWWfqAqDllt3zH52UQ1zVNa44QaVFONaqrhRW-gmt5BNQX-UINqegvVFFBNAdW0gWokiaimNapphWqKqK7IGlTTBqopDNerfU7CQT_8PLRMuxFrjhWTQO23Iz-ImRdhjacOS6WwUxalYIOzQMY8dRJbcub4wheB35aR5ycxTyTjKZxbXOcFOVrna_mSUC-IBQ9iON3YsQsP9-wowEqeHKRix41ekZOKH1MjTq6nYEt3HC_g3H395-k35NEe-SfkCDgi34JlXETvFGx-AX16wrI
linkProvider National Library of Medicine
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Construction+of+Cellulose+Binding+Domain+Fusion+FMN-Dependent+NADH-Azoreductase+and+Glucose+1-Dehydrogenase+for+the+Development+of+Flow+Injection+Analysis+with+Fusion+Enzymes+Immobilized+on+Cellulose&rft.jtitle=Journal+of+applied+glycoscience+%3A+JAG&rft.au=Yano%2C+Shigekazu&rft.au=Hori%2C+Yukari&rft.au=Kijima%2C+Tatsuro&rft.au=Konno%2C+Hiroyuki&rft.date=2019-01-01&rft.pub=Japan+Science+and+Technology+Agency&rft.issn=1344-7882&rft.eissn=1880-7291&rft.volume=66&rft.issue=2&rft.spage=65&rft_id=info:doi/10.5458%2Fjag.jag.JAG-2018_0011&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1344-7882&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1344-7882&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1344-7882&client=summon